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银屑病的新型小分子治疗与新兴生物疗法

Novel Small-Molecule Treatment and Emerging Biological Therapy for Psoriasis.

作者信息

Li Yuanyuan, Cheng Yiheng, Cai Yuchen, Duan Zhenduo, Xu Hong, Huang Yunan, Ma Xiaonan, Xin Xiaofei, Yin Lifang

机构信息

Department of Pharmaceutics, China Pharmaceutical University, Nanjing 210009, China.

The Public Laboratory Platform of China Pharmaceutical University, Nanjing 210009, China.

出版信息

Biomedicines. 2025 Mar 23;13(4):781. doi: 10.3390/biomedicines13040781.

Abstract

Psoriasis is an immune-related disorder that is marked by abnormal thickening of the skin, the rapid multiplication of keratinocytes, and complex interactions between immune cells and the affected areas. Although psoriasis cannot currently be cured, drugs can alleviate symptoms by regulating immune homeostasis and preventing comorbidities. There are many types of drugs to treat psoriasis: small-molecule drugs, including corticosteroids; retinoids; vitamin D analogs; and immunosuppressants, such as glucocorticoid ointment, tretinoin cream, methotrexate tablets, etc. Macromolecular biological drugs, such as Certolizumab, Secukinumab, Guselkumab, etc., include monoclonal antibodies that target various inflammatory signaling pathways. Compared with traditional small-molecule drugs, biological therapies offer better targeting and lower systemic side effects, but their high costs and invasive administration modes constrict their widespread use. Spesolimab is the latest biological agent used to target the interleukin-36 receptor (IL-36R) to be approved for market use, which significantly reduces the risk of general pustular psoriasis (GPP) flare by 84%. Additionally, there are several biological agents used to target the interleukin-23/T helper 17 cell pathway that have already entered Phase II and III clinical trials. At present, the first-line therapeutic strategy for mild psoriasis is topical administration. Systemic therapy and phototherapy are preferred for treating moderate to severe types. However, the current therapeutic drugs for psoriasis cannot completely meet the clinical needs. More advanced drug delivery systems with optimized target effects and better bioavailability are required. Nanocarriers are emerging for the delivery of proteins, nucleic acids, and cell-based therapies. In this review, we analyze the current status of psoriasis therapeutics and discuss novel delivery systems for diverse psoriasis drugs, as well as emerging cell-based therapies. We also summarize the therapeutic effectiveness of different delivery strategies.

摘要

银屑病是一种免疫相关疾病,其特征为皮肤异常增厚、角质形成细胞快速增殖以及免疫细胞与患病区域之间的复杂相互作用。虽然目前银屑病无法治愈,但药物可通过调节免疫稳态和预防合并症来缓解症状。治疗银屑病的药物种类繁多:小分子药物,包括皮质类固醇;维甲酸类;维生素D类似物;以及免疫抑制剂,如糖皮质激素软膏、维甲酸乳膏、甲氨蝶呤片等。大分子生物药物,如赛妥珠单抗、司库奇尤单抗、古塞奇尤单抗等,包括靶向各种炎症信号通路的单克隆抗体。与传统小分子药物相比,生物疗法具有更好的靶向性和更低的全身副作用,但其高昂的成本和侵入性给药方式限制了其广泛应用。司佩索利单抗是最新获批上市的靶向白细胞介素-36受体(IL-36R)的生物制剂,可显著降低泛发性脓疱型银屑病(GPP)发作风险达84%。此外,还有几种靶向白细胞介素-23/辅助性T细胞17细胞途径的生物制剂已进入II期和III期临床试验。目前,轻度银屑病的一线治疗策略是局部给药。中重度类型则首选全身治疗和光疗。然而,目前用于治疗银屑病的药物尚不能完全满足临床需求。需要更先进的具有优化靶向效果和更好生物利用度的药物递送系统。纳米载体正崭露头角,用于蛋白质、核酸和基于细胞的治疗递送。在本综述中,我们分析了银屑病治疗的现状,讨论了多种银屑病药物的新型递送系统以及新兴的基于细胞的疗法。我们还总结了不同递送策略的治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d63c/12025338/22bd62fe05b7/biomedicines-13-00781-g001.jpg

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